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4-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL) CHLOROBENZENE is an organoboron compound that features a chlorobenzene ring connected to a boron-containing heterocycle. It is widely recognized for its role as a fundamental building block in organic synthesis, especially in the creation of carbon-carbon and carbon-heteroatom bonds. 4-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL) CHLOROBENZENE is celebrated for its applications in Suzuki-Miyaura cross-coupling reactions, a technique pivotal in pharmaceutical and material science research. Moreover, it serves as a crucial intermediate in the synthesis of an array of pharmaceuticals, agrochemicals, and materials with promising uses in electronics and optics. Its versatility and stability make it an indispensable asset for chemists in the realm of organic chemistry.

585524-80-7

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585524-80-7 Usage

Uses

Used in Pharmaceutical Industry:
4-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL) CHLOROBENZENE is utilized as a key intermediate in the development of various pharmaceuticals. Its unique structure allows for the formation of complex molecular architectures that are essential in the discovery and synthesis of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL) CHLOROBENZENE is employed as a vital component in the synthesis of agrochemicals. Its reactivity and stability contribute to the production of effective and sustainable solutions for agricultural applications.
Used in Material Science:
4-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL) CHLOROBENZENE is used as a fundamental building block in material science research. Its role in creating carbon-carbon and carbon-heteroatom bonds is crucial for the development of advanced materials with potential applications in various industries.
Used in Electronics:
4-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL) CHLOROBENZENE is leveraged in the electronics industry for its potential applications in the development of electronic materials and devices. Its unique properties make it suitable for use in the creation of components with specific electronic properties.
Used in Optics:
In the field of optics, 4-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL) CHLOROBENZENE is used for its potential applications in the development of optical materials. Its ability to form complex molecular structures makes it a valuable asset in creating materials with tailored optical properties.
Used in Organic Synthesis:
4-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL) CHLOROBENZENE is a versatile building block in organic synthesis, particularly for the formation of carbon-carbon and carbon-heteroatom bonds. Its reactivity and stability make it an essential tool for chemists working on the synthesis of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 585524-80-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,5,5,2 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 585524-80:
(8*5)+(7*8)+(6*5)+(5*5)+(4*2)+(3*4)+(2*8)+(1*0)=187
187 % 10 = 7
So 585524-80-7 is a valid CAS Registry Number.

585524-80-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL) CHLOROBENZENE

1.2 Other means of identification

Product number -
Other names 4-CHLOROPHENYLBORONIC ACID,NEOPENTYL GLYCOL CYCLIC ESTER

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:585524-80-7 SDS

585524-80-7Relevant academic research and scientific papers

Palladium-catalysed reactions of conjugated enyne oxiranes with organoborons: A diastereoselective method of the synthesis of 2,4,5-trienol derivatives

Ziyanak, F?rat,Ku?, Melih,Alkan-Karadeniz, Leman,Artok, Levent

, p. 3652 - 3662 (2018/05/25)

A palladium-catalysed reaction of conjugated enyne oxiranes with organoboron reagents is described. This method allows aryl-substituted vinylallenes containing a hydroxyl group on the allylic position to be synthesized, with good diastereomeric ratios, un

Cu-Catalyzed cross-coupling reactions of epoxides with organoboron compounds

Lu, Xiao-Yu,Yang, Chu-Ting,Liu, Jing-Hui,Zhang, Zheng-Qi,Lu, Xi,Lou, Xin,Xiao, Bin,Fu, Yao

supporting information, p. 2388 - 2391 (2015/02/05)

A copper-catalyzed cross-coupling reaction of epoxides with arylboronates is described. This reaction is not limited to aromatic epoxides, because aliphatic epoxides are also suitable substrates. In addition, N-sulfonyl aziridines can be successfully converted into the products. This reaction provides convenient access to β-phenethyl alcohols, which are valuable synthetic intermediates.

PHARMACEUTICAL USE OF BORONIC ACIDS AND ESTERS THEREOF

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Page 30, (2008/06/13)

Use of compounds to inhibit hormone-sensitive lipase, the use of these compounds as pharmaceutical compositions, pharmaceutical compositions comprising the compounds, method of treatment employing these compounds and compositions, and novel compounds. The present compounds are inhibitors of hormone-sensitve lipase and may be useful in the treatment and/or prevention of a range of medical disorders where a decreased activity of hormone-sensitive lipase is desirable.

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